The following data is part of a premarket notification filed by Biomet Spine Llc. with the FDA for Biomet Spine Fusion System.
| Device ID | K151483 |
| 510k Number | K151483 |
| Device Name: | Biomet Spine Fusion System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Biomet Spine LLC. 310 Interlocken Parkway, Suite 120 Broomfield, CO 80021 |
| Contact | Ted Kuhn |
| Correspondent | Ted Kuhn Biomet Spine LLC. 310 Interlocken Parkway, Suite 120 Broomfield, CO 80021 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-06-02 |
| Decision Date | 2015-07-31 |
| Summary: | summary |